Results 91 to 100 of about 15,429 (247)

Boronate‐Type‐Controlled Regioselective Catalytic [2 + 2 + 2] Cyclotrimerization for Synthesis of Polysubstituted 2‐ and 3‐Borylated Pyridines

open access: yesChemistryEurope
Regioselective synthesis is a crucial concept in organic chemistry, enabling the selective formation of different regioisomers from the same type of starting materials.
Eva Bednářová   +7 more
doaj   +1 more source

Study on the Alkylation Reactions of N(7)-Unsubstituted 1,3-Diazaoxindoles

open access: yesMolecules, 2017
The chemistry of the 5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one (1,3-diazaoxindole) compound family, possessing a drug-like scaffold, is unexplored. In this study, the alkylation reactions of N(7)-unsubstituted 5-isopropyl-1,3-diazaoxindoles bearing ...
Eszter Kókai   +5 more
doaj   +1 more source

An Exploratory Study of the Enzymatic Hydroxycinnamoylation of Sucrose and Its Derivatives

open access: yesMolecules
Phenylpropanoid sucrose esters are a large and important group of natural substances with significant therapeutic potential. This work describes a pilot study of the enzymatic hydroxycinnamoylation of sucrose and its derivatives which was carried out ...
Matej Cvečko   +2 more
doaj   +1 more source

Copper-promoted C5-selective bromination of 8-aminoquinoline amides with alkyl bromides

open access: yesBeilstein Journal of Organic Chemistry
An efficient and practical method for the synthesis of C5-brominated 8-aminoquinoline amides via a copper-promoted selective bromination of 8-aminoquinoline amides with alkyl bromides was developed.
Changdong Shao   +10 more
doaj   +1 more source

Electrochemical Synthesis of Ortho- and Para-Hydroxybenzoic Acids Using CO2: Experimental and Simulation-Based Optimization

open access: yesEngineering Proceedings
The electrochemical conversion of CO2 into value-added aromatic carboxylic acids represents an emerging route for carbon utilization. This work investigates the regioselective electrochemical synthesis of ortho- and para-hydroxybenzoic acids (o-HBA and p-
Bekzod Eshkulov, Ruzimurod Jurayev
doaj   +1 more source

Electrochemical Regioselective Chalcogenocyclizations of 2‐Alkynylbenzamides in Flow

open access: yesChemElectroChem
Electrochemical activation plays a key role in boosting substrate reactivity and directing unique cyclization patterns through the nature of intermediates.
Hanaa Gieman   +2 more
doaj   +1 more source

Using Synthetic Glycans to Investigate Anti‐Glycan Antibodies and Explore Their Medical Potential

open access: yesAngewandte Chemie International Edition, EarlyView.
Anti‐glycan antibodies are essential in health and disease. Access to novel glycan structures paves the way for progress in antibody profiling for biomarker discovery, antibody development, and vaccine design. We summarize the strategies to synthesize and utilize synthetic glycans for the development and application of anti‐glycan antibodies in basic ...
Fabienne Weber   +4 more
wiley   +1 more source

Peptide Thioester and Triazole Derivatives Through On‐Resin Dual‐Modification of Peptide Thiosulfonates

open access: yesAngewandte Chemie International Edition, EarlyView.
An on‐resin dual‐modification strategy for peptides is presented, comprising S‐alkynylation of peptide thiosulfonates and regioselective iridium‐catalyzed azide–thioalkyne cycloaddition. This method reliably provides access to peptides with intricate non‐canonical modifications, being compatible with complex peptides, alkynes and azides.
Marius Werner   +5 more
wiley   +1 more source

The Jekyll and Hyde Nature of Tetrazoles in Polymer Science: From Intrinsic Electronic Duality to Programmable Macromolecular Function

open access: yesAngewandte Chemie International Edition, EarlyView.
Tetrazoles are reframed as substitution‐programmable heterocycles rather than static functional groups in polymer chemistry. By linking electronic identity to synthetic strategy and polymer architecture, this mini‐review establishes a design framework for translating tetrazole duality into predictable macromolecular function.
Meryem S. Akdemir, Hatice Mutlu
wiley   +1 more source

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